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51篇 您的检索式:作者名="FINNING K"
    题名 作者 年代 出处 被引量
1RESEARCH AND SIMULATION OF THE INFLUENCE OF THREE-AXIAL COMPACTION ON POWDER METALLURGIC PRODUCT PROPERTIES显示文摘温暖的粉末压缩过程被有限元素分析软件模仿, MSC/MARC。热机械地联合的分析方法根据更新的 Lagrangian 方法被使用,到模仿温暖的粉末压缩过程。温暖的粉末压缩过程被模仿,并且磨擦状况的影响和紧迫的式样在某些温度在粉末绿色和力学行为的密度上被研究。结果显示为圆柱的协议,与磨擦条件的改进,绿相对密度的分发的一致性是大部分改善了,紧迫的力量和应力减少,并且非一致压过程在某种程度上影响绿密度的分发。穿孔机第一最后压并且死的过程的压力分发的地位出版社与另外的三个过程不同,并且介绍‘ f lume' 的数字。D. G. Wang Y.C. Wu M.H. Jiao T.Xie J.W. Yu K G. Fin 2008Acta Metallurgica Sinica(English Letters)2008,21,2:3
2Use of maternal plasma for noninvasive determina- tion of real RhD status 显示文摘Harper T C Finning K M Martin P 2004Am J Obste Gy- necol2004,191,5:1
3A clinical service in the UK to predict fetal Rh (Rhesus) D blood group using free fetal DNA in maternal plasma 显示文摘Finning K Martin P Daniels G 2004Ann N Y Acad Sci2004,1022,:1
4Fetal sex determination from maternal blood at 6 weeks of gestation when at risk for 21-hydroxylase deficiency显示文摘Bartha JL Fin K Soothill PW 2003Obstet Gynecol2003,101,:1
5Non-invasive fetal sex determination: Impact on clinical practice 显示文摘Finning K M Chitty L S 2008Semin Fetal Neonatal Med2008,13,:1
6Fetal sex determination from maternal blood at 6 weeks of gestation when at risk for 21-hydroxylase deficiency显示文摘Bartha J L Finning K Soothill P W 2003Obstet Gynecol2003,10,52:1
7Fetal genotyping for the K (Kell) and Rh C, c, and E blood groups on cell-free fetal DNA in maternal plasma 显示文摘Finning K Martin P Summers J 2007Transfusion2007,47,11:1
8Fetal RhD genotypingA more efficient use of anti-D immunoglobulin显示文摘Daniels G Finning K Martin P Summers J 2002Transfus Clin Biol2002,14,:1
9Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women:prospective fea-sibility study显示文摘Finning K Martin P Summers J 2008BMJ2008,336,7648:1
10Non-invasive prenatal determination of fetal sex:translating research into clinical practice显示文摘HILL M FINNING K MARTIN P 2011Clin Genet2011,80,1:1
11Fetal blood group genotyping from DNA from maternal plasma:an important advance in the management and prevention of haemolytic disease of the fetus and newborn显示文摘Daniels G Finning K Martin P 2004Vox Sang2004,87,4:1
12De- constructing voltage sensor function and pharmacology in sodi- um channels显示文摘BOSMANS F MAR FIN'IAUCLAIRE M F SWARTZ K J 2008Nature2008,456,7219:1
13The use of maternal plasma for prenatal rhd blood group genotyping显示文摘Finning K Martin P Daniels G 2009Methods Mol Biol2009,496,:1
142001 SCCM/ESICM/ACCP,ATS/SISinternational sepsisdefinitions conference显示文摘Lev y MM Fin k MP Marshall JC et a1 2003Crit Care Med2003,31,5:1
15A clinical service in the Uk to predict fetal Rh (Rhesus) D blood group using free fetal DNA in ma ternal plasma显示文摘Finning K Martin P Daniels G 2004Ann N Y Acad Sci2004,1022,:1
16Fetal RhD genotyping:A more efficient use of anti-D immunoglobulin 显示文摘Daniels G Finning K Martin P 2007Transfus Clin Biol2007,14,7:1
17Non-invasive fetal sex determination: Impact on clinical practice显示文摘Finning K M Chitty L S 2008Semin Fetal Neonatal Med2008,13,2:1
18Non-invasive prenatal determi- nation of fetal sex: translating research into clinieal practice 显示文摘Hill M Finning K Martin P 2011Clin Genet2011,80,1:1
19Fetal blood group genotyping from DNA from maternal plasma: an important advance in the management and prevention of haemolytic disease of the fetus and newborn 显示文摘Daniels G Finning K Martin P 2004Vox Sang2004,87,4:1
20Non-invasive prenatal determination of fetal sex: translating research into clinical practice显示文摘Hill M Finning K Martin P 2011Clin Genet2011,80,1:1
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